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ORTHOPAEDICS e II: SPINE AND PELVIS

Discitis and spinal involves a pus-producing infection of the disc and vertebrae. It can
be considered that spondylitis, discitis and spondylodiscitis are a
continuum of the same process.1 This clinical spectrum can also
infection involve primary or more commonly secondary epidural abscess,
pyogenic facet joint septic arthritis and vertebral osteomyelitis.
Edward Matthews
Oliver Stokes Classification and epidemiology
Spinal infection can be characterized by the immune reaction to
the causative organism. In the developed world the majority
Abstract cause a pyogenic reaction. The developing world has a higher
Spinal infection poses a diagnostic challenge and a low threshold for burden of disease from Mycobacterium tuberculosis (TB) and
investigation should be maintained. Presentation is varied and non- zoonotic infections.
specific symptoms mean that patients are investigated by many spe- Meticillin sensitive Staphylococcus aureus (MSSA) is the
cialities. The majority of spinal infection is from haematogenous most common organism isolated (63%) and along with
spread and therefore an origin of infection needs to be sought. Treat- Streptococcus species (20%)1 cause the majority of infections.
ment of spondylodiscitis is routinely managed by non-surgical treat- However, in 25e33% of patients no pathogen is isolated.1,2 Other
ment with a prolonged period of antibiotics. Complications of typical organisms include Gram negative bacilli, commonly seen
spondylodiscitis can lead to morbidity and may be difficult to treat in infections secondary to intravenous drug abuse. Salmonella
and often require surgery. It is essential to attempt to obtain microbi- infection is more common in those patients with immune
ological diagnosis. Initial management and investigation does affect compromise and sickle cell anaemia.2 Table 1 provides a list of
treatment strategies and it is important to understand this. commonly encountered pathogens and their prevalence.
Keywords Discitis; epidural abscess; osteomyelitis; spinal infection; Granulomatous discitis occurs most commonly from M.
spondylodiscitis; vertebral tuberculosis (TB) and brucellosis. These combined with Candida
spp. and other fungal infections cause significant morbidity and
mortality in the immunosuppressed and in the developing world.
Introduction Brucella infection, a zoonosis, occurs secondary to consuming
unpasteurized dairy products or occupational exposure to
Adult spinal infection is an uncommon clinical condition and has
infected animals.
the potential to cause a spectrum of morbidity and occasionally
Spondylodiscitis accounts for a small burden of disease in the
mortality. This article provides the reader with an understanding
developed healthcare system and has been reported to represent
of spinal infection and an update on current guidelines and
2e7% of all cases of osteomyelitis.2 The burden of spondylo-
evidence-based best practice.
discitis is reported to have an incidence of 3.7/100,000 per year
Spinal infections can range from indolent to rapidly indolent
according to recent UK-based study.3
or rapidly destructive. Immunocompromised patients are
Factors that increase this risk of developing discitis in the UK
particularly at risk, and spinal infections can present to a wide
are widely reported to be diabetes mellitus, steroid use and
range of surgical and medical specialities. The natural history of
immunosuppression, intravenous drug abuse, malnutrition and
the disease is dependent on host, pathogen and comorbid vari-
renal failure. These are summarized in Box 1. Tuberculosis and
ables and can lead to progressive destruction which if untreated
human immunodeficiency virus (HIV) pose a significant burden
can result in significant deformity, neural compromise and death.
of disease in the developing world. Pyogenic spondylitis is more
The clinical picture on presentation or diagnosis affects subse-
common in the elderly, whereas epidural abscess is more of a
quent investigation and management. Therefore, thorough
problem with disseminated bacteraemia and iatrogenic causes.
assessment of these patients is essential. Spinal infections most
Hadjipavlou et al.1 found septicaemia to be the biggest risk factor
often occur due to haematogenous spread of infection from
for spondylodiscitis, with tobacco and intravenous drug use
elsewhere in the body; de novo spinal infection is rare, therefore
being the next most common risk factor (Table 1 and Box 1).
multisystem assessment of these patients is important.
There are a number of descriptive medical names that are
Pathogenesis
synonymous for the same clinical entity. Discitis refers to an
infective condition of the intervertebral disc. Commonly this is The aetiology of spinal infection is either haematogenous spread,
used to describe pyogenic spondylodiscitis, taking the prefix from iatrogenic or contiguous. Haematogenous infection can be
the Greek, spondylos, for vertebra, a clinical condition that disseminated by either the arterial tree or the venous system.
This is the most commonly encountered source in clinical prac-
tice. The arterial vascular supply to the spine is via segmental
arteries. The intervertebral disc itself is avascular (in adults). The
Edward Matthews FRCS(Tr & Orth) is a Trauma and Orthopaedic vertebral endplate, however, is vascularized, allowing for direct
Specialist Registrar in the South West Deanery, UK. Conflicts of extension from endplate to disc, hence the surrounding end
interest: none. plates are involved in cases of discitis, leading to the term
Oliver Stokes FRCS (Tr & Orth) MSc is a Consultant Spinal Surgeon at spondylodiscitis the term spondylodiscitis is often used. Prostatic
the Royal Devon and Exeter Hospital, Exeter, UK. Conflicts of biopsy can lead to a venous source of infection via the valveless
interest: none. vertebral veins of Batson. Infective endocarditis and urinary tract

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ORTHOPAEDICS e II: SPINE AND PELVIS

They also recommended that neurological symptoms with


Pathogens1,4e7 fever should prompt urgent investigation.8
Organisms Percentages Risk factor Unremitting pain is a significant feature and is present in 90% of
presentations.2 Red flag symptoms should specifically be elicited
Staphylococcus sp. 63e20 and if present result in expedited investigation and treatment. Box 2
MSSA 36e21 Surgery is a commonly described red flag symptoms that should be spe-
MRSA 14e7 Elderly cifically asked for in the history; it is not exhaustive but does
Coagulase negative 3e16 Device related prompt suspicion for consideration of serious diagnoses. The
staphylococci presence of neurological deficit is a bad prognostic sign and implies
Streptococcus spp 19e6 a compressive or vascular lesion and should arouse suspicion of an
Escherichia coli 11e4 UTI epidural abscess, it should be treated as a surgical emergency.
Pseudomonas aeruginosa 6e3 IVDU Neurological deficit is present in one-third of patients with an
Salmonella spp. 2 Sickle cell epidural abscess.2 Epidural abscesses, either primary or sec-
Propionibacterium sp. 1 Postoperative ondary from spondylodiscitis, are reported to be present in 35%
Brucellosis 21e48 Developing world e of all spinal pyogenic infections.1 Severe neurological deficits are
unpasteurized goats milk present in 37%, including paraplegia or paralysis; with surgical
Tuberculosis 9e46 Developing world decompression only 23% of those make complete recovery.2
No organism cultured 24 Postoperative infection has a quoted incidence of 2% following
lumbar discectomy.9 The most common presentation of these
IVDU, intravenous drug use; MRSA, meticillin sensitive Staphylococcus aureus;
MSSA, meticillin sensitive Staphylococcus aureus; UTI, urinary tract infection. cases are acute postoperative surgical site infections, with the
characteristic signs of acute inflammation, wound discharge and
Table 1 raised inflammatory markers. These cases are a distinct group
from other causes of discitis and should be managed aggressively
with a low threshold for debridement and intervention. Further
detail on postoperative discitis is beyond the scope of this article.
Risk factors for discitis
Examine for the presence of deformity, para-spinal spasm and
referred pain. Examination findings should demonstrate or
C Intravenous drug abuse
exclude fever and systemic sepsis. If a large collection is also
C Elderly
present, then psoas and a para-spinal abscess may co-exist.
C Chronic renal failure including renal replacement therapy
Document the extent of neurological deficit. The examination
C Infective endocarditis
should be repeated at regular intervals. Progressive neurological
C Diabetes mellitus
deterioration requires emergency surgical intervention. The
C Steroids & immunosuppression
American Spinal Injury Association impairment scale is a useful
C Malnutrition
tool for confirming the neurological deficit and charting any
C Tuberculosis and human immunodeficiency virus
progression.10
Box 1
Investigation
infection have been reported to be present in 12e17% of spon- Initial investigation guides early management of disease process.
dylodiscitis diagnoses, respectively.7 The recommended initial diagnostic tests include the presence of
Iatrogenic infection complicates 1e15% of lumbar spine sur- raised inflammatory markers and positive results of magnetic
geries. Risk factors include diabetes, revision surgery and post- resonance scanning of the whole spine.
operative haematoma. Epidural anaesthesia and lumbar punc- Testing for raised inflammatory markers has a low cost and
ture also expose patients to the risk of discitis, as do spinal cord has been shown to have a sensitivity of 94e100%.8 Obtaining
stimulators.
Direct or contiguous spread is rare. It can occur with cases of
mycotic aneurysm, oesophageal pathology, retropharyngeal ab- Red flag signs
scess and intraabdominal sepsis.
C Weight loss
Presentation C Thoracic back pain
C Sphincter dysfunction
Diagnosis of spondylodiscitis requires a high index of suspicion. C Neurological deficit
Delay in treatment may cause significant complications and C Age <20 or >55 years
morbidity. Recent guidance5 from the Infectious Diseases Society C Known history malignancy or trauma
of America (IDSA) suggests that the diagnosis should be sus- C Night pain or non-mechanical pain
pected in those with: C Fever
 new or worsening back pain C Corticosteroid use or immunosuppression
 back pain associated with fever or raised inflammatory C Structural deformity
markers or recent staph aureus infection/infective endo-
carditis/septicaemia. Box 2

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ORTHOPAEDICS e II: SPINE AND PELVIS

a culture of the causative organism guides effective treatment


and influences prognosis. It is for this reason that the two sets of
bacterial blood cultures (both aerobic and anaerobic) are rec-
ommended when the diagnosis of spondylodiscitis is
considered.8
It is commonly accepted that prior to starting empiric antibi-
otics, the responsible organism is cultured. Blood culture is an
inexpensive and effective method of obtaining this. If this fails to
yield a culture, then a percutaneous biopsy is recommended.
However, when the patient has a significant infection the ability
to safely delay treatment to obtain a microbiological diagnosis
should be abandoned if there is evidence of:
 systemic sepsis
 haemodynamic instability
 neurological compromise/cauda equina syndrome (where
immediate surgical decompression is undertaken).
The use of antibiotics reduces the microbiological yield of
biopsy and blood culture and for this reason and in the absence
of the clinical scenarios above it is common practise to withhold
antibiotic use until a microbiological sample is obtained.
Magnetic resonance imaging (MRI) is the radiological investi-
gation of choice to help make the diagnosis. MRI is widely avail-
able during working hours and has a sensitivity of 97%, specificity
of 93%, and an accuracy of 94% in diagnosing spondylodiscitis.8
MRI can also differentiate between infective and neoplastic pro-
cesses. Where negative, and the diagnosis of discitis is still
strongly suspected, a serial or follow up scan is recommended at a
3-week intervals. Figure 1 shows the T2 mid sagittal sequence of
spondylodiscitis at L4/5 which demonstrates the hyper-intense
signal in T2 and also demonstrates epidural abscess posteriorly.
Figure 2 shows the T1 mid sagittal sequence of multilevel thoracic
discitis with fluid collection anteriorly to this.
 The specific findings on MRI in spondylodiscitis is the high Figure 1 T2 mid-sagittal sequence of spondylodiscitis at L4/5.
signal on T2-weighted images and confluence of disc space
and vertebral marrow on T1 images
 Sub-ligamentous spread and the involvement of more than
three vertebral levels is suggestive of tuberculous
infection11
The use of contrast agents can be helpful in some circum-
stances. Gadolinium-based contrast MR imaging can be useful in
the differentiation of infected granulation tissue from abscess.
The contrast will show a peri-abscess halo of intense signal
surrounding an area of low signal that will not be present in
granulation tissue. The use of gadolinium, as with all contrast,
comes with the risk of nephritis and therefore should be used
with appropriate caution after considering the risks and benefits.
Computed tomography has a significant role to play where
biopsy is required. Image-guided aspiration is recommended
where the causative organism has not been confirmed by either
blood cultures or serological testing.8 It is advised against when
there is a positive bacteraemia involving S. aureus, Staphylo-
coccus lugdenesis or Brucella. Biopsy results should be sent for
microbiological culture and pathological review to exclude
neoplastic process.
Bone scanning can be combined with gallium scans to give a
sensitive investigation of >90% for discitis where MRI cannot be Figure 2 T1 mid-sagittal sequence of multilevel thoracic discitis with
employed. White-cell labelled scanning is not recommend.8 fluid collection.

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ORTHOPAEDICS e II: SPINE AND PELVIS

Plain radiographs are not useful in the acute diagnostic work Bracing
up; it is widely accepted that there is a period of 4 weeks in which Orthotic use in spinal infection has a limited evidence base.
radiographic signs will not be present in spondylodiscitis, if at Where the presence of infection leads to deformity and spinal
all. The common findings are a destructive process that is centred instability the use of an orthotic is likely to be insufficient apart
around the disc space, i.e. the superior endplate and the inferior from a temporary device to give comfort, and not as a long-term
end of the vertebral body above. Due to a destructive appear- solution. Surgery for kyphosis and pseudarthrosis provides a
ance, it is also important to rule out a neoplastic process and a better outcomes and lower pain scores.1
myeloma screen including serum electrophoresis and urinary
Bence-Jones proteins to diagnose myeloma should be performed. Surveillance
It is important to consider the aetiology of discitis when a Patients should be reviewed regularly to evaluate clinical
diagnosis is established. Careful evaluation of risk factors could improvement in pain and systemic symptoms. Clinical exami-
point to infective endocarditis, intravenous catheter infection, nation should also be regularly repeated to assess for neurolog-
solid organ abscess and haemodialysis, all of which have sig- ical sequelae and development of deformity. The use of serial
nificant morbidity and mortality if not recognized and treated. inflammatory markers is widely reported but there is limited
evidence on to how to interpret slowly declining CRP. It has been
Management reported that a CRP of 27.5 mg/l at 4 weeks could be a predictive
marker of how effective treatment is but there is a paucity of
The management can be complex and needs tailoring to the evidence for this.6
patient’s clinical picture.
Outcomes
Antibiotics
The mainstay of treatment is a course of intravenous antibiotics If patients suffer from a complication of discitis they have a poorer
until inflammatory markers are on a downward trend and outcome. The potential for paralysis and deformity pose signifi-
heading towards a C-reactive protein (CRP) below 50 mg/l. cant morbidity. Absolute failure can cause, at best, deformity and
CRP of less than 30 mg/l is common around the 4-week point, pain with ongoing osteomyelitis and, at worst, it can cause death
following treatment, according to Sur et al.3 There is also no from sepsis. Figure 2 demonstrates an inadequately treated spinal
consensus on the length of intravenous therapy and on the infection in a patient showing significant destruction and
conversion to oral therapy. There is evidence that 6 weeks of deformity.
antibiotic therapy has no inferiority to 3 months of antibiotics.12 Epidural abscess formation secondary to discitis is a common
The current consensus on empirical antibiotic therapy is that complication of infection, affecting 35% in one series,1 and one-
there should be careful evaluation of patient background, past third these cases were associated with paralysis.
medical history and social and geographic susceptibility.8 Where Mortality from discitis is rare. A recent case series from
fungal or mycobacterial pathogens are suspected there is a Madrid reported a mortality of 7/108 (6.5%).14 The 1-year
limited role for empirical therapy. mortality has been reported to be 11%,15 but attributing this
The main pyogenic organisms are MSSA, meticillin resistant mortality rate solely to discitis is difficult due to the underlying
S. aureus (MRSA) and streptococcal species and Gram negative comorbidities present in many affected patients. Comorbid pa-
species; local empiric guidance will involve broad-spectrum an- tients represent the more likely to be affected and they are likely
tibiotics until culture positive guidance agent can be employed. to have the worst outcomes.

Surgical intervention Conclusion


There is limited evidence-based guidance to guide surgical
Spinal infection is a condition that presents to many specialities
management of spinal infection. The indications emergency
and in many clinical entities, without pathognomonic clinical
decompression and washout include:
symptoms or signs. Detection requires a high index of suspicion.
 systemic toxicity from sepsis
Initial management has significant implications as to subsequent
 progressive neurological compromise (including cauda
treatment. Poorly treated spondylodiscitis can have serious
equina syndrome and cord compression).
consequences and morbidity and therefore is best performed by a
Indications for less emergent surgical intervention include:
multidisciplinary team of physicians, surgeons, radiologists and
 medical comorbidity with inadequate response to medical
microbiologists. A
therapy - percutaneous washout with Jamshidi needle
 vertebral collapse
 unremitting back pain and nerve root/foraminal REFERENCES
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 progressive deformity. togenous pyogenic spinal infections and their surgical manage-
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